Canonical Allele Identifier: CA898240530
Community Standard Title: NC_000003.12:g.12447383G>T
Gene: PPARG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12447383G>T , CM000665.2:g.12447383G>T GRCh38
NC_000003.11:g.12488882G>T , CM000665.1:g.12488882G>T GRCh37
NC_000003.10:g.12463882G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011533842.1:c.1271-23438G>T XP_011532144.1:n.1271-23438G>T
XM_011533842.2:c.1271-23438G>T XP_011532144.1:n.1271-23438G>T
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